A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525064



Internal ID15452357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107739156..107742077hg38UCSC Ensembl
Innerchr9:110501437..110504358hg19UCSC Ensembl
Innerchr9:109541258..109544179hg18UCSC Ensembl
Innerchr9:107580992..107583913hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382922
hg192922
hg182922
hg172922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701116
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525064
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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